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Endothelial cell study in a case of Werner's syndrome undergoing phacoemulsification and Yettrium-Aluminum-Garnet laser capsulotomy.
[werner syndrome]
Werner
's
syndrome
(
WS
)
is
a
rare
autosomal
recessive
disorder
with
multisystem
manifestations
of
premature
aging
from
the
second
decade
of
life
.
Cataract
is
one
of
the
features
of
WS
.
Cataract
surgery
is
complicated
with
postoperative
wound
dehiscence
and
bullous
keratopathy
when
the
surgery
is
done
by
intracapsular
or
conventional
extracapsular
method
.
We
report
the
short
-term
result
of
phacoemulsification
and
Neodymimum
Yettrium-
Aluminum-
Garnet
laser
(
Nd
YAG
)
capsulotomy
in
a
case
of
WS
with
bilateral
cataracts
.
Postoperatively
and
post
capsulotomy
,
there
was
no
change
in
the
endothelial
cell
morphology
.
There
was
an
8
.
6
%
decrease
in
endothelial
cell
count
at
the
end
of
15
months
postoperatively
and
11
months
post
YAG
capsulotomy
.
This
decrease
is
within
the
acceptable
range
of
cell
loss
after
phacoemulsification
and
YAG
capsulotomy
.
To
the
best
of
our
knowledge
,
this
is
the
first
reported
case
of
YAG
laser
capsulotomy
in
WS
.
Diseases
Validation
Diseases presenting
"first reported case"
symptom
achondroplasia
acute rheumatic fever
alexander disease
allergic bronchopulmonary aspergillosis
aniridia
cutaneous mastocytosis
dedifferentiated liposarcoma
epidermolysis bullosa simplex
fabry disease
focal myositis
harlequin ichthyosis
heparin-induced thrombocytopenia
kabuki syndrome
malignant atrophic papulosis
megacystis-microcolon-intestinal hypoperistalsis syndrome
pleomorphic liposarcoma
primary hyperoxaluria type 1
thoracic outlet syndrome
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wolf-hirschhorn syndrome
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